Canonical Allele Identifier: CA2343274019
Gene: TNNI3 HGNC NCBI

Linked Data

dbSNP Id: rs920524388
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154650A>C , CM000681.2:g.55154650A>C GRCh38
NC_000019.9:g.55666018A>C , CM000681.1:g.55666018A>C GRCh37
NC_000019.8:g.60357830A>C NCBI36
NG_007866.2:g.8083T>G , LRG_432:g.8083T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.372+91T>G MANE Select ENSP00000341838.5:n.372+91T>G
ENST00000665070.1:c.405+58T>G ENSP00000499482.1:n.405+58T>G
ENST00000344887.9:c.372+91T>G ENSP00000341838.5:n.372+91T>G
ENST00000585806.5:n.371+91T>G
ENST00000586669.5:n.380+91T>G
ENST00000587176.5:n.647T>G
ENST00000588882.1:c.297+91T>G ENSP00000466729.1:n.297+91T>G
NM_000363.4:c.372+91T>G , LRG_432t1:c.372+91T>G NP_000354.4:n.372+91T>G
NM_000363.5:c.372+91T>G MANE Select NP_000354.4:n.372+91T>G
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